Chemical Analyst on site

Avantor; Carnaxide; On-site; EUR 27,000 - 38,000; Full time

Benefits offered by this job

20 days leave

Bridge days

Free meals

Health insurance

Life insurance

Job summary

Avantor seeks a Chemical Analyst / Onsite Specialist I to support day-to-day lab operations on-site at Recipharm in Queluz de Baixo, near Lisbon. This hands-on role emphasizes maintaining smooth workflows, compliance with quality standards, and strong collaboration with a customer site team.

The candidate will perform routine testing, manage consumables, and document results while communicating updates to stakeholders.

Qualifications

• 3–5 years of experience in a laboratory, QC, or regulated operations.
• High school diploma or GED required; science degree preferred.
• Experience in pharmaceutical or manufacturing-adjacent labs is an advantage.
• Familiarity with laboratory consumables, utilities, and equipment.

Responsibilities

• Support daily laboratory operations at Recipharm site in Queluz de Baixo, in line with SOPs.
• Minimize laboratory workflow interruptions through operational and technical support.
• Perform routine chemical or biological testing and support quality control activities, including sampling.
• Perform analytical testing using chromatographic techniques (HPLC and/or GC).
• Manage laboratory consumables and utilities (gas cylinders, liquids, dry ice, buffers, solvents, LN2).
• Collect, document, and organize laboratory data and observations.
• Maintain accurate laboratory documentation and records.
• Communicate updates and service metrics to internal teams and stakeholders.
• Assist with day-to-day troubleshooting and issue resolution.

Skills

Organizational skills

Communication skills

Independent work

Customer-facing

Education

High school diploma or GED

Tools

HPLC

GC

Job description

The Opportunity

Executes day‑to‑day lab operations & support objectives at customer facilities, following a varied set of procedures, focused on minimizing laboratory workflow interruptions. Problems and issues are typically less concrete and frequently changing, and are solved by applying experience from comparable situations in the past and/or selecting solutions within known alternatives. Tasks include end-to-end management of gas cylinders and liquid tanks, dry ice, and instrument buffers, solvents and liquid nitrogen, and supporting quality control workflows by executing sampling. Collects, documents, and organizes data and observations. Communicates activity records, service level metrics and other information requiring explanation or interpretation to team members, supervisors or customers.

Job Type: Full‑Time

Department: Laboratory Operations (LPS)

Location: Queluz de Baixo (Lisbon area), Portugal

We are looking for a Chemical Analyst / Onsite Specialist I to support day‑to‑day laboratory operations on‑site at Recipharm in Queluz de Baixo, a leading pharmaceutical manufacturing partner located in the Lisbon area. This is a hands‑on, customer‑embedded role focused on ensuring smooth laboratory workflows, operational continuity, and compliance with quality and safety standards in a regulated environment.

Key Responsibilities

• Support daily laboratory operations at the Recipharm site in Queluz de Baixo, in line with established SOPs
• Proactively minimize laboratory workflow interruptions through operational and technical support
• Perform routine chemical or biological testing and support quality control activities, including sampling
• Perform analytical testing using chromatographic techniques (e.g. HPLC and/or GC)
• Manage laboratory consumables and utilities, including gas cylinders, liquid tanks, dry ice, buffers, solvents, and liquid nitrogen
• Collect, document, and organize laboratory data and observations
• Maintain accurate laboratory documentation and records
• Communicate operational updates, activity records, and service metrics to internal teams and Recipharm stakeholders
• Support routine troubleshooting and resolution of day‑to‑day laboratory issues

Requirements

• High school diploma or GED required; degree in a scientific discipline preferred
• 3–5 years of experience in a laboratory, QC, or regulated operational environment
• Experience working in pharmaceutical or manufacturing‑adjacent laboratories is an advantage
• Familiarity with laboratory consumables, utilities, and equipment
• Experience with HPLC and/or GC is a plus
• Strong organizational and communication skills
• Ability to work independently in a customer‑facing, on‑site role

Benefits

• 20 days of annual leave in the first year, 22 days in subsequent years (+ up to 3 additional days based on attendance)
• 3 bridge days per year
• Free meals provided in the on‑site canteen
• Company‑funded health insurance for the employee and family
• Company‑funded life insurance

Why Join This Role

• Work directly on‑site at Recipharm in Queluz de Baixo (Lisbon area)
• Be part of a dedicated LPS team embedded with the customer
• Gain exposure to laboratory operations, QC workflows, and customer collaboration
• Stable, long‑term position aligned with an ongoing service contract

Disclaimer

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

EEO Statement

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.

If you need a reasonable accommodation for any part of the employment process, please contact us by email at [e-mail] and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case‑by‑case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.